US11192088B2ActiveUtilityA1
Superabsorbent polymer and method for preparing the same
Est. expiryDec 23, 2035(~9.5 yrs left)· nominal 20-yr term from priority
C08K 2201/003C08F 20/06C08F 220/385C08K 7/26C08K 3/34B01J 20/267C08K 3/36C08J 3/24C08J 3/075B01J 20/3021C08J 3/12A61L 15/60C08K 7/00B01J 20/28007C08J 2333/02C08F 2/10C08F 20/56C08K 2201/005B01J 20/28085C08J 9/04C08F 222/102C08L 33/02C08F 220/06
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Claims
Abstract
The present invention relates to superabsorbent polymer having an improved absorption speed through micropores formed inside, and a method for preparing the same.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1. A superabsorbent polymer, comprising:
a base resin powder comprising a crosslinked homopolymer of acrylic acid monomers having acid groups of which at least a part are neutralized,
wherein a plurality of pores with a diameter of 1 μm or more are formed in the base resin powder,
wherein the crosslinked homopolymer comprises layered silicate-based particles dispersed in a crosslinking structure,
wherein the layered silicate-based particles comprise hectorite,
wherein the superabsorbent polymer has a time for removing vortex generated of 60 seconds or less when stirring 2 grams of the superabsorbent polymer at 600 rpm in 50 ml of a 0.9 wt % NaCl solution, and
wherein a centrifuge retention capacity for a saline solution, measured according to EDANA method WSP 241.2, is 45 g/g or more.
2. The superabsorbent polymer according to claim 1 , wherein the plurality of pores with a diameter of 1 μm or more formed in the base resin powder comprise micropores with diameters of 10 μm to 100 μm.
3. The superabsorbent polymer according to claim 1 , wherein the layered silicate-based particles comprise a unit crystal comprising a metal oxide layer, and a silica layer comprising silica formed on at least one side of the metal oxide layer.
4. The superabsorbent polymer according to claim 1 , wherein the layered silicate-based particles have a column structure with a maximum diameter of a cross section of 1 nm to 100 nm, and a height of 0.1 nm to 20 nm.
5. The superabsorbent polymer according to claim 1 , wherein the layered silicate-based particles are included in the content of 0.01 parts by weight to 5 parts by weight, based on 100 parts by weight of the base resin powder.
6. The superabsorbent polymer according to claim 1 , wherein the crosslinked homopolymer comprises a crosslinking structure in which polymer chains of the acrylic acid monomers are crosslinked through crosslinkable functional groups of an internal crosslinking agent.
7. The superabsorbent polymer according to claim 1 , wherein the crosslinked homopolymer comprises a crosslinked homopolymer formed by polymerization of the acrylic acid monomers in the presence of an internal crosslinking agent comprising a multifunctional acrylate-based compound.
8. The superabsorbent polymer according to claim 6 , wherein the internal crosslinking agent comprises one or more selected from the group consisting of polyethyleneglycol diacrylate(PEGDA), glycerin diacrylate glycerin triacrylate, non-modified or ethoxylated trimethylol propane triacrylate(TMPTA), hexanedioldiacrylate, and triethyleneglycol diacrylate.
9. A method for preparing a superabsorbent polymer comprising steps of:
conducting a crosslinking polymerization of acrylic acid monomers having acid groups of which at least a part are neutralized, in the presence of layered silicate-based particles comprised hectorite, a blowing agent and an internal crosslinking agent, to form a hydrogel polymer; and
drying, grinding and sieving the hydrogel polymer to form a base resin powder, wherein the superabsorbent polymer comprises:
the base resin powder comprising a crosslinked homopolymer of the acrylic acid monomers having acid groups of which at least a part are neutralized,
wherein a plurality of pores with a diameter of 1 μm or more are formed in the base resin powder,
wherein the crosslinked homopolymer comprises the layered silicate-based particles dispersed in a crosslinking structure,
wherein the superabsorbent polymer has a time for removing vortex generated of 60 seconds or less when stirring 2 grams of the superabsorbent polymer at 600 rpm in 50 ml of a 0.9 wt % NaCl solution, and
wherein a centrifuge retention capacity for a saline solution, measured according to EDANA method WSP 241.2, is 45 g/g or more.
10. The method for preparing superabsorbent polymer according to claim 9 , wherein, in the step of forming the hydrogel polymer, based on 100 parts by weight of the blowing agent, 1 to 1000 parts by weight of the layered silicate-based particles are used.
11. The method for preparing superabsorbent polymer according to claim 9 , wherein the step of forming hydrogel polymer comprises steps of
forming a first solution comprising the internal crosslinking agent, and the acrylic acid monomers having acid groups of which at least a part are neutralized;
forming a second solution comprising the layered silicate-based particles and the blowing agent; and
progressing the crosslinking polymerization of a monomer composition comprising the first solution and the second solution.
12. The method for preparing superabsorbent polymer according to claim 11 , wherein, in the step of forming the first solution comprising the internal crosslinking agent, and the acrylic acid monomers having acid groups of which at least a part are neutralized, the content of the internal crosslinking agent is 0.01 parts by weight to 5 parts by weight, based on 100 parts by weight of the acrylic acid monomers.
13. The method for preparing superabsorbent polymer according to claim 11 , wherein, in the step of crosslinking polymerization of a monomer composition comprising the first solution and the second solution, the content of the second solution is 1 part by weight to 100 parts by weight, based on 100 parts by weight of the first solution included in the monomer composition.
14. The superabsorbent polymer according to claim 7 , wherein the internal crosslinking agent comprises one or more selected from the group consisting of polyethyleneglycol diacrylate(PEGDA), glycerin diacrylate glycerin triacrylate, non-modified or ethoxylated trimethylol propane triacrylate(TMPTA), hexanedioldiacrylate, and triethyleneglycol diacrylate.Cited by (0)
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